38644-10-9

Basic information

• Product Name: [2-chloro-6-(trifluoromethyl)phenanthren-9-yl](piperidin-2-yl)methanol
• CAS NO: 38644-10-9
• Molecular Formula: C₂₁H₁₉ClF₃NO
• Molecular Weight: 393.8299
• Mol File: 38644-10-9.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 418.9°C at 760 mmHg
• Flash Point: 207.1°C
• Density: 1.345g/cm³
• Vapor Pressure: 9.15E-08mmHg at 25°C
• Refractive Index: 1.618
• CAS DataBase Reference: [2-chloro-6-(trifluoromethyl)phenanthren-9-yl](piperidin-2-yl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: [2-chloro-6-(trifluoromethyl)phenanthren-9-yl](piperidin-2-yl)methanol(38644-10-9)
• EPA Substance Registry System: [2-chloro-6-(trifluoromethyl)phenanthren-9-yl](piperidin-2-yl)methanol(38644-10-9)

Safety Data

• Hazardous Substances Data: 38644-10-9(Hazardous Substances Data)

Usage

Description

[2-chloro-6-(trifluoromethyl)phenanthren-9-yl](piperidin-2-yl)methanol is a complex organic chemical compound characterized by a phenanthrene ring with a chloro and trifluoromethyl group at the 2 and 6 positions, respectively. It features a piperidin-2-yl group at the 9 position, which is connected to the phenanthrene ring through a methanol group. [2-chloro-6-(trifluoromethyl)phenanthren-9-yl](piperidin-2-yl)methanol is of interest in pharmaceutical research and drug development due to the presence of the bioactive piperidin-2-yl group and the unique chemical properties conferred by the chloro and trifluoromethyl groups.

Uses

Used in Pharmaceutical Research and Drug Development:
[2-chloro-6-(trifluoromethyl)phenanthren-9-yl](piperidin-2-yl)methanol is used as a chemical intermediate for the synthesis of novel bioactive molecules and pharmaceutical compounds. The presence of the piperidin-2-yl group, which is commonly found in various pharmaceuticals, makes this compound a promising candidate for the development of new drugs with potential therapeutic applications.
Used in Medicinal Chemistry:
[2-chloro-6-(trifluoromethyl)phenanthren-9-yl](piperidin-2-yl)methanol is utilized in medicinal chemistry for the exploration of its unique chemical properties and reactivity. The chloro and trifluoromethyl groups may offer specific advantages in the design and synthesis of new chemical entities with improved pharmacological profiles. Further study and research on [2-chloro-6-(trifluoromethyl)phenanthren-9-yl](piperidin-2-yl)methanol could lead to the discovery of innovative therapeutic agents with enhanced efficacy and selectivity.